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NSAIDs and opioids 63<br />

For now, with a few possible exceptions such as arthritis pain (see p. 00),<br />

we recommend ED providers avoid use of the COX-2 selective NSAIDs. <strong>This</strong><br />

general recommendation is subject to modification in particular clinical<br />

circumstances, as outlined in other chapters of this text. Further data<br />

will undoubtedly clarify the role of COX-2 selective NSAIDs for acute (and<br />

chronic) analgesia.<br />

If the side effects of the COX-2 selective NSAIDs require further elucidation,<br />

there is much less uncertainty about risks associated with nonselective<br />

NSAIDs. Among the issues to consider are GI bleeding, renal insufficiency,<br />

and impaired fracture healing. These complications, which are less likely<br />

with a few days’ use than with longer NSAID prescription, should inform – but<br />

not dominate – emergency physicians’ drug decision-making. 10 Despite the<br />

well-characterized NSAID risks, this class is still often the best choice for ED<br />

patients. One reason is that the usual alternatives include agents with known<br />

adverse effects of their own (e.g. opioids), or drugs with lesser analgesic<br />

efficacy (e.g. acetaminophen).<br />

The gastrointestinal risks of NSAIDs are reduced by co-administration of<br />

gastroprotective therapy such as misoprostol or, preferably, proton pump<br />

inhibitors. 11,12 Commentators supporting the use of proton pump inhibitors<br />

in patients receiving NSAIDs cite data showing that, compared with NSAID<br />

monotherapy, the dual-therapy approach reduces GI bleed incidence by<br />

over 80%. 13 Pharmaco-economic analysis suggests that, for short-course<br />

therapy prescribed from the ED, the combination will usually be more cost<br />

effective than COX-2 selective NSAID monotherapy. 14<br />

Perhaps surprisingly for many conditions described in this text, the combination<br />

of NSAIDs and opioids fails to accrue additive (or synergistic) analgesic<br />

results. The point is illustrated by recent data from a study of children with<br />

suspected fractures. The authors of the study found that children with mild-tomoderate<br />

pain responded equally well to ibuprofen (10 mg/kg PO), oxycodone<br />

(0.1 mg/kg PO), or the combination of the two, and preferred monotherapy for<br />

reasons of safety and simplicity. 15 The message for the ED physician is that<br />

single-drug therapy may be best. Do not assume that NSAID-associated risks –<br />

however small in an individual patient – are outweighed by analgesic benefit in<br />

a patient who is already going to be taking opioids.

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